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Ureidoacetic acid

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Identification
Molecular formula
C3H6N2O3
CAS number
496-46-8
IUPAC name
2-ureidoacetic acid
State
State

At room temperature, ureidoacetic acid is in a solid state.

Melting point (Celsius)
198.00
Melting point (Kelvin)
471.15
Boiling point (Celsius)
315.00
Boiling point (Kelvin)
588.15
General information
Molecular weight
118.09g/mol
Molar mass
118.0880g/mol
Density
1.5634g/cm3
Appearence

The compound has a white crystalline appearance. It is typically found as a powder.

Comment on solubility

Solubility of 2-Ureidoacetic Acid

2-Ureidoacetic acid, with the chemical formula C3H6N2O3, exhibits interesting solubility characteristics that are important for various applications. Understanding its solubility can be crucial for fields such as pharmaceuticals and biochemistry.

Key points about the solubility of 2-ureidoacetic acid:

  • Water Solubility: This compound is generally highly soluble in water due to the presence of multiple polar functional groups, which facilitate hydrogen bonding with water molecules.
  • Organic Solvents: It may show variable solubility in organic solvents; however, its solubility is usually lower compared to water, reflecting its polar nature.
  • Influencing Factors: Factors such as pH and temperature can significantly affect the solubility of 2-ureidoacetic acid, especially given its acidic properties.

As a result, 2-ureidoacetic acid can be classified as a polar compound with a strong tendency to dissolve in aqueous environments. This solubility property is essential to consider for its potential uses in various biochemical and industrial processes.

Interesting facts

Interesting Facts About 2-Ureidoacetic Acid

2-Ureidoacetic acid, also known as ureidoacetate, is a fascinating compound that plays a significant role in various biochemical processes. Here are some intriguing aspects to consider:

  • Biological Significance: This compound is known to be integral in the metabolism of certain amino acids, acting as a substrate in various enzymatic reactions.
  • Precursor to Other Compounds: 2-Ureidoacetic acid serves as a precursor to several important biological molecules, highlighting its relevance in synthetic biology and pharmacology.
  • Therapeutic Potential: Due to its unique structure, this compound has been studied for its potential applications in drug development, particularly for conditions related to amino acid metabolism.
  • Research and Development: Ongoing research is exploring the use of 2-ureidoacetic acid in the synthesis of new compounds that may have significant therapeutic effects.

As a chemistry student or scientist, you may find it particularly interesting that ureidoacetate can exhibit a variety of functional activities, contributing to its potential use in medicinal chemistry. The diverse functional groups present within its molecular structure lend themselves to various interactions with biological systems, emphasizing the importance of understanding such compounds in the broader context of biochemical research.

In summary, the study of 2-ureidoacetic acid not only enhances our understanding of metabolic pathways but also opens doors to novel therapeutic strategies, making it a compound worthy of further exploration.

Synonyms
Hydantoic acid
462-60-2
N-Carbamoylglycine
Carbamoylglycine
Glycoluric acid
2-(carbamoylamino)acetic acid
N-Carbamylglycine
Acetic acid, ureido-
Glycine, N-(aminocarbonyl)-
2-Ureidoacetic acid
Urea, (carboxymethyl)-
Carbomoylglycine
ureidoacetic acid
Glycine, N-carbamoyl-
N-Carboxymethylurea
Acetic acid, ((aminocarbonyl)amino)-
NSC 49417
CCRIS 6533
EINECS 207-328-5
CB 1636
BRN 1812022
[(aminocarbonyl)amino]acetic acid
Q4F314U63K
MFCD00047876
NSC-49417
N-(CARBOXYMETHYL)UREA
DTXSID7060045
CHEBI:133351
4-04-00-02411 (Beilstein Handbook Reference)
carbamyl-glycine
carbamoyl glycine
N-carbamoyl glycine
Acetic acid, [(aminocarbonyl)amino]-
NCarbamylglycine
UNII-Q4F314U63K
NCarbamoylglycine
N-carbamyl glycine
Acetic acid, ureido
HydantoinsA currencyure
Urea, (carboxymethyl)
Glycine, N(aminocarbonyl)
Oprea1_578490
SCHEMBL289921
DTXCID4040478
Glycine, Ncarbamoyl (7CI,8CI)
Glycine, N-carbamoyl-(7CI,8CI)
NSC49417
Acetic acid, ((aminocarbonyl)amino)
STL553754
AKOS000264528
AT23074
AS-56566
SY051314
DB-026618
DB-051365
CS-0204817
H0655
NS00031593
EN300-10397
AB00981907-01
Q27286991
Z57009586
InChI=1/C3H6N2O3/c4-3(8)5-1-2(6)7/h1H2,(H,6,7)(H3,4,5,8
207-328-5